Allele Registry

Canonical Allele Identifier: PA2826629283

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491517

RCV000759147

RCV000797850

RCV003316642

RCV003464057

RCV004003460

ClinVar Variation:

428382

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe1193Ser	CA46719891 NM_001281492.2:c.3578T>C